Lifileucel, the first commercial TIL therapy for advanced melanoma, has been approved by the FDA, marking a major advance in personalized cancer treatment.
The recent approval of lifileucel by the U.S. Food and Drug Administration marks a significant milestone as the first commercial tumor-infiltrating lymphocyte (TIL) therapy for advanced melanoma. This development represents a major advancement in cancer therapy. In a new commentary published in Cancer Cell, scientists from the Moffitt Cancer Center provide a detailed overview of the therapy's development and emphasize its transformative potential (1✔ ✔Trusted Source
Tumor-Infiltrating Lymphocyte Therapy Marks a Milestone in Cancer Treatment
Go to source). "TIL therapy represents a major advancement in personalized cancer treatment, offering new possibilities for patients with treatment-resistant cancers," said Amod Sarnaik, M.D., lead author and senior member of the Cutaneous Oncology Department at Moffitt.
‘Lifileucel's approval opens new frontiers in treating advanced melanoma, with a significant reduction in dropout rates during treatment. #cancerresearch #medindia’
The Journey of Tumor-Infiltrating Lymphocyte Therapy
Tumor-infiltrating lymphocyte therapy has been under development for several decades. Its journey began with preclinical studies at the National Cancer Institute (NCI) in the early 1980s. James J. Mulé, Ph.D., a renowned immunologist and the associate center director of Translational Science at Moffitt, introduced TIL research to the cancer center in 2003. Since then, Moffitt has been instrumental in advancing and validating this innovative immunotherapy.In 2010, Moffitt opened its first TIL trials, the first center outside of the NCI to treat patients with the investigational therapy. This initial study, treating 13 patients with advanced metastatic melanoma, yielded promising results: five responses, including two complete responses lasting beyond five years. The commentary examines Moffitt’s subsequent clinical trials, which aimed to address the high dropout rate due to disease progression during TIL manufacturing. These trials combined TIL therapy with newly approved anti-melanoma agents, significantly reducing the dropout rate from 32% to 5%.
A New Era in Personalized Cancer Treatment
Moffitt is also working on the next generation of TIL therapy. Shari Pilon-Thomas, Ph.D., and other immunologists at the center are investigating innovative ways to stimulate and improve TIL therapy growth and manufacturing and determine the best infusion timing to ensure optimal patient outcomes. Moffitt researchers are also expanding this therapeutic approach to treat other solid tumor cancer types, such as lung, sarcoma, cervical and bladder.“We are at the beginning of unlocking the potential of T-cell and cell therapies for treating advanced cancers. The FDA’s approval of lifileucel is a monumental step to inspire further investment and innovation in T-cell therapies, particularly TIL therapy,” said Moffitt President and CEO Patrick Hwu, M.D. “Our pioneering research at Moffitt into next-generation TIL therapies aims to extend these lifesaving treatments to a broader range of cancer patients.”
Reference:
- Tumor-Infiltrating Lymphocyte Therapy Marks a Milestone in Cancer Treatment - (https://www.moffitt.org/newsroom/news-releases/tumor-infiltrating-lymphocyte-therapy-marks-a-milestone-in-cancer-treatment/)
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